<p>The histograms show the ratio of average expression levels between individuals with and without the CNV for all genes inside a CNV region. The shift between the two distributions is significantly larger than would be expected by chance (MWU: ).</p
<p>Each part of the figure shows the graphical representation of the first two eigenvectors after PC...
<p>*Statistically significant (multiple-testing corrected p-value<0.05) deviations from the expected...
<p>There were 205 ACC (panel A), 82 ACC-PLUS (panel B), 123 ACC-ONLY (panel C), 180 CBLH (panel D), ...
<p>The table shows the distribution of CNV patterns among haplogroups for ten variants that showed o...
<p>Common CNV with significant difference in allele frequencies compare to the HapMap3 dataset.</p
<p>(<b>A</b>) Proportion of deletions (white) and duplications (black) overlapping four mutually exc...
<p>In case informative polymorphic genotypes are present <i>between</i> haplotypes in an individual,...
Understanding the genetic contribution to phenotype variation of human groups is necessary to elucid...
Understanding the genetic contribution to phenotype variation of human groups is necessary to elucid...
Background: Understanding the genetic contribution to phenotype variation of human groups is necessa...
<p>The color bar on the right shows the color codes assigned to each frequency range in percent.</p
BACKGROUND:Understanding the genetic contribution to phenotype variation of human groups is necessar...
Copy-number variants (CNVs) form an abundant class of genetic variation with a presumed widespread i...
Recently, the extent of copy number variation (CNV) throughout the genome has been shown to be far g...
<p><b>(A)</b> Allele frequency spectrum of bi-allelic CNVs across all 66 individuals, showing most d...
<p>Each part of the figure shows the graphical representation of the first two eigenvectors after PC...
<p>*Statistically significant (multiple-testing corrected p-value<0.05) deviations from the expected...
<p>There were 205 ACC (panel A), 82 ACC-PLUS (panel B), 123 ACC-ONLY (panel C), 180 CBLH (panel D), ...
<p>The table shows the distribution of CNV patterns among haplogroups for ten variants that showed o...
<p>Common CNV with significant difference in allele frequencies compare to the HapMap3 dataset.</p
<p>(<b>A</b>) Proportion of deletions (white) and duplications (black) overlapping four mutually exc...
<p>In case informative polymorphic genotypes are present <i>between</i> haplotypes in an individual,...
Understanding the genetic contribution to phenotype variation of human groups is necessary to elucid...
Understanding the genetic contribution to phenotype variation of human groups is necessary to elucid...
Background: Understanding the genetic contribution to phenotype variation of human groups is necessa...
<p>The color bar on the right shows the color codes assigned to each frequency range in percent.</p
BACKGROUND:Understanding the genetic contribution to phenotype variation of human groups is necessar...
Copy-number variants (CNVs) form an abundant class of genetic variation with a presumed widespread i...
Recently, the extent of copy number variation (CNV) throughout the genome has been shown to be far g...
<p><b>(A)</b> Allele frequency spectrum of bi-allelic CNVs across all 66 individuals, showing most d...
<p>Each part of the figure shows the graphical representation of the first two eigenvectors after PC...
<p>*Statistically significant (multiple-testing corrected p-value<0.05) deviations from the expected...
<p>There were 205 ACC (panel A), 82 ACC-PLUS (panel B), 123 ACC-ONLY (panel C), 180 CBLH (panel D), ...
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